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Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations

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Acknowledgements

We would like to thank Prof. Douglas Higgs, Director, and Dr. Noemi Roy, MRC Molecular Haematology Unit, MRC Weatherall Institute of Molecular Medicine, University of Oxford (UK) for NGS and helping for analysis. This study was performed with the support of the Indian Council of Medical Research, New Delhi.

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Authors and Affiliations

  1. Department of Haematogenetics, National Institute of Immunohaematology, Indian Council of Medical Research, 13th Floor, New Multistoried Building, K.E.M Hospital Campus, Parel, Mumbai, 400012, India

    Prabhakar Kedar, Vaishali Parmar, Rati Devendra, Vinod Gupta, Prashant Warang & Manisha Madkaikar

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  1. Prabhakar Kedar
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  2. Vaishali Parmar
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  3. Rati Devendra
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  4. Vinod Gupta
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  5. Prashant Warang
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  6. Manisha Madkaikar
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Correspondence to Prabhakar Kedar.

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Kedar, P., Parmar, V., Devendra, R. et al. Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations. Ann Hematol 96, 2135–2139 (2017). https://doi.org/10.1007/s00277-017-3116-5

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  • DOI: https://doi.org/10.1007/s00277-017-3116-5

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